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  2. Neurofibromatosis - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis

    Neurofibromatosis type I is the most common of the three types and is caused by genetic changes in the NF1 gene located on chromosome 17 (17q11.2). This gene encodes a cytoplasmic protein known the neurofibromin, which functions as a tumor suppressor and therefore serves as a signal regulator of cell proliferation and differentiation.

  3. Neurofibromatosis type I - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis_type_I

    Café au lait spot characteristic of NF1 Diagnostic criteria of neurofibromatosis type I, requiring at least 2 of the mentioned items. [6]The following is a list of conditions and complications associated with NF-1, and, where available, age range of onset and progressive development, occurrence percentage of NF-1 population, method of earliest diagnosis, and treatments and related medical ...

  4. Crowe sign - Wikipedia

    en.wikipedia.org/wiki/Crowe_sign

    The Crowe sign or Crowe's sign is the presence of axillary (armpit) freckling in people with neurofibromatosis type I (von Recklinghausen's disease). These freckles occur in up to 30% of people with the disease and their presence is one of six diagnostic criteria for neurofibromatosis.

  5. Neurofibromatosis type II - Wikipedia

    en.wikipedia.org/wiki/Neurofibromatosis_type_II

    Neurofibromatosis type II (also known as MISME syndrome – multiple inherited schwannomas, meningiomas, and ependymomas) is a genetic condition that may be inherited or may arise spontaneously, and causes benign tumors of the brain, spinal cord, and peripheral nerves. The types of tumors frequently associated with NF2 include vestibular ...

  6. Neurofibroma - Wikipedia

    en.wikipedia.org/wiki/Neurofibroma

    A neurofibroma is a benign nerve-sheath tumor in the peripheral nervous system.In 90% of cases, they are found as stand-alone tumors (solitary neurofibroma, solitary nerve sheath tumor [1] or sporadic neurofibroma [1]), while the remainder are found in persons with neurofibromatosis type I (NF1), an autosomal-dominant genetically inherited disease.

  7. “My Disability Has Opened Doors”: Actor Adam ... - AOL

    www.aol.com/disability-opened-doors-actor-adam...

    NF1 is a common form of neurofibromatosis, accounting for 96% of cases.It affects an estimated 1 in 3,000 births worldwide annually, as per the Cleveland Clinic.. It has “variable manifestations ...

  8. Neurofibromin - Wikipedia

    en.wikipedia.org/wiki/Neurofibromin

    Main symptoms of neurofibromatosis type I [28] Mutations in NF1 are primarily associated with neurofibromatosis type 1 (NF1, also known as von Recklinghausen syndrome). [6] [7] NF1 is the most common single gene disorder in humans, occurring in about 1 in 2500–3000 births worldwide. [29]

  9. Phakomatosis - Wikipedia

    en.wikipedia.org/wiki/Phakomatosis

    Main symptoms of neurofibromatosis type I. [7] Diagnostic criteria of neurofibromatosis type I, requiring at least 2 of the mentioned items. [8] Neurofibromatosis type 1 is the most common phakomatosis and it affects approximately 1 in 2500-3000 live births. [9] It is a genetic disorder due to a germline mutation in the NF1 gene.

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